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Synergy between stimulator cells in the induction of the anti-Mlsa response.

作者信息

DeKruyff R H, Laning J, Dorf M E

机构信息

Children's Hospital, Stanford, Palo Alto, CA 94305.

出版信息

J Immunogenet. 1988 Feb-Jun;15(1-3):135-43. doi: 10.1111/j.1744-313x.1988.tb00415.x.

Abstract

We have identified two types of clones responsive to Mls determinants. One type responded vigorously to purified B cells from mice bearing Mlsa-stimulatory determinants. The other type, including clone Ly1-N5, responded vigorously to unfractionated spleen cells, but failed to respond to B cells alone or to spleen-adherent cells (SAC) alone from the Mlsa-bearing mice. Synergy between two stimulator cell types, B cells and SAC, was required to induce the Mls response of clone Ly1-N5. The failure of clone Ly1-N5 to respond to Mlsa-bearing B cells was reversed by the addition of SAC taken from mice bearing the Mlsa allele or the non-stimulatory Mlsb allele. B cells were required to provide the Mlsa determinant. The Mls response of clone Ly1-N5 is restricted by class II determinants shared by the H-2b, H-2d and H-2k haplotypes, but not the H-2q haplotype. The optimal response of the clone was obtained by using B cells bearing both Mlsa and the permissive H-2 alloantigen. However, complementation was also observed between B cells bearing Mlsa and the non-permissive Iaq and SAC bearing the nonstimulatory Mlsb, but a permissive Ia epitope, resulting in activation of the clone. Clone Ly1-N5 responds to Mlsa-bearing B cells only in the presence of SAC.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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Synergy between stimulator cells in the induction of the anti-Mlsa response.
J Immunogenet. 1988 Feb-Jun;15(1-3):135-43. doi: 10.1111/j.1744-313x.1988.tb00415.x.

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